SG172386A1 - Purification of recombinantly produced interferon - Google Patents
Purification of recombinantly produced interferon Download PDFInfo
- Publication number
- SG172386A1 SG172386A1 SG2011046687A SG2011046687A SG172386A1 SG 172386 A1 SG172386 A1 SG 172386A1 SG 2011046687 A SG2011046687 A SG 2011046687A SG 2011046687 A SG2011046687 A SG 2011046687A SG 172386 A1 SG172386 A1 SG 172386A1
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- SG
- Singapore
- Prior art keywords
- ifn
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- Prior art date
Links
- 108010050904 Interferons Proteins 0.000 title claims abstract description 57
- 102000014150 Interferons Human genes 0.000 title claims abstract description 57
- 229940079322 interferon Drugs 0.000 title claims abstract description 41
- 238000000746 purification Methods 0.000 title description 10
- 108010029485 Protein Isoforms Proteins 0.000 claims abstract description 315
- 102000001708 Protein Isoforms Human genes 0.000 claims abstract description 315
- 238000010828 elution Methods 0.000 claims abstract description 261
- 238000000034 method Methods 0.000 claims abstract description 73
- 238000005349 anion exchange Methods 0.000 claims abstract description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 104
- 239000000243 solution Substances 0.000 claims description 104
- 239000001488 sodium phosphate Substances 0.000 claims description 66
- 229910000162 sodium phosphate Inorganic materials 0.000 claims description 64
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 64
- 229910019142 PO4 Inorganic materials 0.000 claims description 56
- 239000010452 phosphate Substances 0.000 claims description 56
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 55
- 239000011780 sodium chloride Substances 0.000 claims description 52
- 238000004587 chromatography analysis Methods 0.000 claims description 39
- 239000007983 Tris buffer Substances 0.000 claims description 27
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 27
- 238000011068 loading method Methods 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 20
- 239000012160 loading buffer Substances 0.000 claims description 17
- 239000003957 anion exchange resin Substances 0.000 claims description 11
- 239000007853 buffer solution Substances 0.000 claims description 11
- 229920002271 DEAE-Sepharose Polymers 0.000 claims description 9
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 5
- 238000005571 anion exchange chromatography Methods 0.000 claims description 4
- 241000894006 Bacteria Species 0.000 claims description 3
- 108010047761 Interferon-alpha Proteins 0.000 claims description 3
- 102000006992 Interferon-alpha Human genes 0.000 claims description 3
- 102100040018 Interferon alpha-2 Human genes 0.000 claims 13
- 108010079944 Interferon-alpha2b Proteins 0.000 claims 13
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 claims 1
- 230000002051 biphasic effect Effects 0.000 abstract description 28
- 238000004440 column chromatography Methods 0.000 abstract 1
- 235000011008 sodium phosphates Nutrition 0.000 description 58
- 239000000872 buffer Substances 0.000 description 52
- 239000012149 elution buffer Substances 0.000 description 40
- 238000002360 preparation method Methods 0.000 description 32
- 102000004169 proteins and genes Human genes 0.000 description 25
- 108090000623 proteins and genes Proteins 0.000 description 25
- 150000003839 salts Chemical class 0.000 description 24
- 230000000694 effects Effects 0.000 description 21
- 238000000926 separation method Methods 0.000 description 21
- 229940047124 interferons Drugs 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 13
- 238000004007 reversed phase HPLC Methods 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 238000010561 standard procedure Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000008363 phosphate buffer Substances 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 238000011098 chromatofocusing Methods 0.000 description 8
- 230000003247 decreasing effect Effects 0.000 description 8
- 101001042415 Cratylia mollis Mannose/glucose-specific lectin Cramoll Proteins 0.000 description 7
- 238000002835 absorbance Methods 0.000 description 7
- 239000006174 pH buffer Substances 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000003111 delayed effect Effects 0.000 description 6
- 229920001184 polypeptide Polymers 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 102000004196 processed proteins & peptides Human genes 0.000 description 6
- 108090000765 processed proteins & peptides Proteins 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 102100029775 Eukaryotic translation initiation factor 1 Human genes 0.000 description 5
- 101001012787 Homo sapiens Eukaryotic translation initiation factor 1 Proteins 0.000 description 5
- 101000643378 Homo sapiens Serine racemase Proteins 0.000 description 5
- 238000003556 assay Methods 0.000 description 5
- AIXMJTYHQHQJLU-UHFFFAOYSA-N chembl210858 Chemical compound O1C(CC(=O)OC)CC(C=2C=CC(O)=CC=2)=N1 AIXMJTYHQHQJLU-UHFFFAOYSA-N 0.000 description 5
- 239000000356 contaminant Substances 0.000 description 5
- 150000001413 amino acids Chemical class 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- 241000588724 Escherichia coli Species 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 229920002684 Sepharose Polymers 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 238000004220 aggregation Methods 0.000 description 3
- 125000003275 alpha amino acid group Chemical group 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 239000006167 equilibration buffer Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000012064 sodium phosphate buffer Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 239000008366 buffered solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000013375 chromatographic separation Methods 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- -1 e.g. Proteins 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 239000011534 wash buffer Substances 0.000 description 2
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 108010077805 Bacterial Proteins Proteins 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 241000206602 Eukaryota Species 0.000 description 1
- 238000010268 HPLC based assay Methods 0.000 description 1
- 102000008070 Interferon-gamma Human genes 0.000 description 1
- 108010074328 Interferon-gamma Proteins 0.000 description 1
- 108010044467 Isoenzymes Proteins 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 125000000729 N-terminal amino-acid group Chemical group 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical group CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 1
- 239000012564 Q sepharose fast flow resin Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001028 anti-proliverative effect Effects 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 239000012062 aqueous buffer Substances 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229960003130 interferon gamma Drugs 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 238000010369 molecular cloning Methods 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 201000006417 multiple sclerosis Diseases 0.000 description 1
- OHDXDNUPVVYWOV-UHFFFAOYSA-N n-methyl-1-(2-naphthalen-1-ylsulfanylphenyl)methanamine Chemical compound CNCC1=CC=CC=C1SC1=CC=CC2=CC=CC=C12 OHDXDNUPVVYWOV-UHFFFAOYSA-N 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000012610 weak anion exchange resin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/555—Interferons [IFN]
- C07K14/56—IFN-alpha
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14036108P | 2008-12-23 | 2008-12-23 | |
| PCT/US2009/068433 WO2010075159A1 (en) | 2008-12-23 | 2009-12-17 | Purification of recombinantly produced interferon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG172386A1 true SG172386A1 (en) | 2011-08-29 |
Family
ID=41650422
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2011046687A SG172386A1 (en) | 2008-12-23 | 2009-12-17 | Purification of recombinantly produced interferon |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20110257368A1 (zh) |
| EP (1) | EP2382237A1 (zh) |
| JP (1) | JP2012513200A (zh) |
| CN (1) | CN102264761A (zh) |
| AU (1) | AU2009330278B2 (zh) |
| CA (1) | CA2746502A1 (zh) |
| MX (1) | MX2011006762A (zh) |
| SG (1) | SG172386A1 (zh) |
| WO (1) | WO2010075159A1 (zh) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2021258734A1 (en) * | 2020-04-20 | 2023-01-05 | Altum Pharmaceuticals Inc. | Recombinant interferon |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT72322B (en) | 1980-01-08 | 1982-09-23 | Biogen Nv | Process for preparation of recombinant dna molecules and of polipeptides similar to human interferon |
| US4530901A (en) | 1980-01-08 | 1985-07-23 | Biogen N.V. | Recombinant DNA molecules and their use in producing human interferon-like polypeptides |
| US4456748A (en) | 1981-02-23 | 1984-06-26 | Genentech, Inc. | Hybrid human leukocyte interferons |
| US4414150A (en) | 1980-11-10 | 1983-11-08 | Genentech, Inc. | Hybrid human leukocyte interferons |
| US4315852A (en) | 1980-11-26 | 1982-02-16 | Schering Corporation | Extraction of interferon from bacteria |
| US4364863A (en) | 1980-12-29 | 1982-12-21 | Schering Corporation | Extraction of interferon from bacteria |
| US4678751A (en) | 1981-09-25 | 1987-07-07 | Genentech, Inc. | Hybrid human leukocyte interferons |
| US6936694B1 (en) | 1982-05-06 | 2005-08-30 | Intermune, Inc. | Manufacture and expression of large structural genes |
| US4534906A (en) | 1982-11-01 | 1985-08-13 | Genentech, Inc. | Removal of impurities from human leukocyte interferon preparations |
| US4432895A (en) | 1982-11-24 | 1984-02-21 | Hoffmann-La Roche Inc. | Monomeric interferons |
| CA1231306A (en) * | 1983-03-03 | 1988-01-12 | Erich Hochuli | Purification of interferon |
| DE3410439A1 (de) | 1984-03-22 | 1985-09-26 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-on-2,2-dioxid und dessen nichttoxischen salzen sowie der dabei als zwischenprodukt(e) auftretenden acetoacetamind-n-sulfonsaeure(salze) |
| US5196323A (en) * | 1985-04-27 | 1993-03-23 | Boehringer Ingelheim International Gmbh | Process for preparing and purifying alpha-interferon |
| WO1989003225A1 (en) * | 1987-10-06 | 1989-04-20 | Interferon Sciences, Inc. | Purification of monomeric interferon |
| US4765903A (en) | 1987-10-06 | 1988-08-23 | Interferon Sciences, Inc. | Purification of monomeric interferon |
| FR2628744B1 (fr) * | 1988-03-18 | 1991-07-26 | Agronomique Inst Nat Rech | Isoformes de la trophoblastine, nouveaux interferons constitues par lesdites isoformes, leurs procedes d'obtention et leurs applications |
| DK0679718T3 (da) | 1994-04-09 | 2001-10-22 | Hoffmann La Roche | Fremgangsmåde til fremstilling af alfa-interferon |
| ES2348104T3 (es) * | 1998-11-12 | 2010-11-30 | Schering Corporation | Metodo para la conversion de isoformas de interferon y productos de las mismas. |
| EP1556498A1 (en) | 2002-11-01 | 2005-07-27 | Cadila Healthcare Ltd. | Method for producing recombinant human interferon alpha 2b polypeptide in pichia pastoris |
-
2009
- 2009-12-17 AU AU2009330278A patent/AU2009330278B2/en not_active Ceased
- 2009-12-17 SG SG2011046687A patent/SG172386A1/en unknown
- 2009-12-17 MX MX2011006762A patent/MX2011006762A/es active IP Right Grant
- 2009-12-17 EP EP09796544A patent/EP2382237A1/en not_active Withdrawn
- 2009-12-17 WO PCT/US2009/068433 patent/WO2010075159A1/en active Application Filing
- 2009-12-17 JP JP2011542426A patent/JP2012513200A/ja active Pending
- 2009-12-17 US US13/141,269 patent/US20110257368A1/en not_active Abandoned
- 2009-12-17 CN CN2009801522434A patent/CN102264761A/zh active Pending
- 2009-12-17 CA CA2746502A patent/CA2746502A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| MX2011006762A (es) | 2011-07-20 |
| AU2009330278B2 (en) | 2013-01-31 |
| CN102264761A (zh) | 2011-11-30 |
| CA2746502A1 (en) | 2010-07-01 |
| JP2012513200A (ja) | 2012-06-14 |
| EP2382237A1 (en) | 2011-11-02 |
| AU2009330278A1 (en) | 2010-07-01 |
| US20110257368A1 (en) | 2011-10-20 |
| WO2010075159A1 (en) | 2010-07-01 |
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